1. Metabolic Enzyme/Protease Vitamin D Related/Nuclear Receptor Immunology/Inflammation NF-κB
  2. Endogenous Metabolite LXR Fatty Acid Synthase (FASN) Interleukin Related Reactive Oxygen Species NOD-like Receptor (NLR)
  3. Desmosterol

Desmosterol is a cholesterol-like molecule. In the Bloch pathway of cholesterol biosynthesis, Desmosterol is a direct precursor of cholesterol. As an endogenous metabolite, Desmosterol is used to study cholesterol metabolism . Desmosterol is an LXR activator and SREBP inhibitor, which can suppress macrophage inflammasome activation and prevent vascular inflammation and atherosclerosis. A reduction in Desmosterol promotes the production of mitochondrial reactive oxygen species (ROS) in macrophages and pyrin domain-dependent inflammasome activation of NLRP3. Desmosterol holds potential for research in inflammation, metabolism, and cardiovascular diseases .

For research use only. We do not sell to patients.

Desmosterol Chemical Structure

Desmosterol Chemical Structure

CAS No. : 313-04-2

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Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMF
ready for reconstitution
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Based on 5 publication(s) in Google Scholar

Other Forms of Desmosterol:

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Description

Desmosterol is a cholesterol-like molecule. In the Bloch pathway of cholesterol biosynthesis, Desmosterol is a direct precursor of cholesterol. As an endogenous metabolite, Desmosterol is used to study cholesterol metabolism [1]. Desmosterol is an LXR activator and SREBP inhibitor, which can suppress macrophage inflammasome activation and prevent vascular inflammation and atherosclerosis. A reduction in Desmosterol promotes the production of mitochondrial reactive oxygen species (ROS) in macrophages and pyrin domain-dependent inflammasome activation of NLRP3. Desmosterol holds potential for research in inflammation, metabolism, and cardiovascular diseases [1][2][3].

IC50 & Target[1]

Human Endogenous Metabolite

 

Cellular Effect
Cell Line Type Value Description References
A549 ED50
> 50 μg/mL
Compound: 1, desmosterol
Cytotoxicity against human A549 cells by MTT assay
Cytotoxicity against human A549 cells by MTT assay
[PMID: 8984148]
HT-29 ED50
> 50 μg/mL
Compound: 1, desmosterol
Cytotoxicity against human HT29 cells by MTT assay
Cytotoxicity against human HT29 cells by MTT assay
[PMID: 8984148]
KB ED50
> 50 μg/mL
Compound: 1, desmosterol
Cytotoxicity against human KB cells by MTT assay
Cytotoxicity against human KB cells by MTT assay
[PMID: 8984148]
P388 ED50
33.53 μg/mL
Compound: 1, desmosterol
Cytotoxicity against mouse P388 cells by MTT assay
Cytotoxicity against mouse P388 cells by MTT assay
[PMID: 8984148]
In Vitro

Desmosterol depletion (by activating the DHCR24 gene in Dhcr24TG mice to lower Desmosterol levels in macrophages for 4 weeks) inhibits LXR activation, upregulates immune response genes, suppresses cholesterol efflux, thereby leading to lipid accumulation in macrophages and foam cell formation, which is closely associated with the development of atherosclerosis disease [2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Western Blot Analysis[3]

Cell Line: Mouse peritoneal macrophages (TGEM) and human hepatocyte cell line (HepG2)
Concentration: 10 μM
Incubation Time: 48 hours
Result: Activated Abca1 protein expression in TGEMs but had no significant effect in HepG2 cells.

Real Time qPCR[3]

Cell Line: Mouse peritoneal macrophages (TGEM)
Concentration: 10 μM
Incubation Time: 48 h
Result: Suppressed the expression of the SREBP target gene Dhcr24.
In Vivo

Desmosterol depletion (by intraperitoneal injection of Adenovirus (AAV-Cre) to activate the DHCR24 gene in Dhcr24TG mice, thereby reducing Desmosterol levels in macrophages) would suppress LXR activation, upregulate immune response genes, inhibit cholesterol efflux, leading to lipid accumulation in macrophages and foam cell formation, which is closely associated with the development of atherosclerosis disease [2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Dhcr24TG and WT mice
Note:
1. Dhcr24TG mice: Crossing Dhcr24fl/fl mice with LysM-Cre mice to obtain conditional Dhcr24TG mice, ensuring that DHCR24 was overexpressed only in macrophages
2. DHCR24 catalyzed the final step in the conversion of Desmosterol to cholesterol. Activating the DHCR24 gene decreased the level of Desmosterol.
Dosage: This experiment did not involve drug administration but altered Desmosterol levels through genetic engineering:
1. Adenovirus (AAV-Cre) was injected (i.p.) to activate DHCR24 in Dhcr24fl/fl mice.
2. After genetic modification, macrophages were isolated from blood and analyzed via Western Blot after 2 weeks of AAV-Cre injection.
Administration: Samples of macrophages were collected starting from 2 weeks after the virus injection, with the total experimental period lasting 4 weeks.
Result: Significantly reduced the LXR signaling in Dhcr24TG mice, and downregulated LXR-dependent genes like ABCA1 and ABCG1 (Desmosterol depletion).
Increased expression of inflammatory genes like Cxcl9, Cxcl10, Il6 in Dhcr24TG macrophages.
Molecular Weight

384.64

Formula

C27H44O

CAS No.
Appearance

Solid

Color

White to off-white

SMILES

C/C(C)=C\CC[C@@H](C)[C@H]1CC[C@@]2([H])[C@]3([H])CC=C4C[C@@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C

Structure Classification
Initial Source
Shipping

Room temperature in continental US; may vary elsewhere.

Storage

-20°C, sealed storage, away from moisture

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

Solvent & Solubility
In Vitro: 

DMF : 50 mg/mL (129.99 mM; Need ultrasonic)

H2O : < 0.1 mg/mL (insoluble)

Preparing
Stock Solutions
Concentration Solvent Mass 1 mg 5 mg 10 mg
1 mM 2.5998 mL 12.9992 mL 25.9983 mL
5 mM 0.5200 mL 2.5998 mL 5.1997 mL
View the Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

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Purity & Documentation

Purity: ≥98.0%

References

Complete Stock Solution Preparation Table

* Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
DMF 1 mM 2.5998 mL 12.9992 mL 25.9983 mL 64.9958 mL
5 mM 0.5200 mL 2.5998 mL 5.1997 mL 12.9992 mL
10 mM 0.2600 mL 1.2999 mL 2.5998 mL 6.4996 mL
15 mM 0.1733 mL 0.8666 mL 1.7332 mL 4.3331 mL
20 mM 0.1300 mL 0.6500 mL 1.2999 mL 3.2498 mL
25 mM 0.1040 mL 0.5200 mL 1.0399 mL 2.5998 mL
30 mM 0.0867 mL 0.4333 mL 0.8666 mL 2.1665 mL
40 mM 0.0650 mL 0.3250 mL 0.6500 mL 1.6249 mL
50 mM 0.0520 mL 0.2600 mL 0.5200 mL 1.2999 mL
60 mM 0.0433 mL 0.2167 mL 0.4333 mL 1.0833 mL
80 mM 0.0325 mL 0.1625 mL 0.3250 mL 0.8124 mL
100 mM 0.0260 mL 0.1300 mL 0.2600 mL 0.6500 mL
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    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Desmosterol
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HY-113224
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